Senior GRC Consultant consulting clients on GRC software RiMaGo and implementing risk strategies. Collaborating with development team and conducting training sessions in GRC.
AC
Hybrid Oncology Research Regulatory Specialist
Posted 4 months ago
About the role
- Oncology Research Regulatory Specialist managing regulatory documents and compliance for clinical trials. Supporting a multidisciplinary team within Avera Cancer Institute.
Responsibilities
- Works under general direction to perform professional level clinical research assignments.
- Prepares and completes regulatory documents for protocols as requested by investigators, sub-investigators and clinical research coordinators.
- Submits all required research documents to the protocol sponsor, the Institutional Review Boards (IRB), the FDA, and any other regulatory agency as required by the research project.
Requirements
- 2 years regulatory, quality or data analyst experience.
- Bachelor's degree preferred.
- 1-3 years related research experience and/or training.
Benefits
- PTO available day 1 for eligible hires.
- Up to 5% employer matching contribution for retirement.
- Career development guided by hands-on training and mentorship.
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